Artificial neural networks for the inverse design of nanoparticles with preferential nano-bio behaviors

摘要

Safe and efficient use of ultrasmall nanoparticles (NPs) in biomedicine requires numerous independent conditions to be met, including colloidal stability, selectivity for proteins and membranes, binding specificity, and low affinity for plasma proteins. The ability of a NP to satisfy one or more of these requirements depends on its physicochemical characteristics, such as size, shape, and surface chemistry. Multiscale and pattern recognition techniques are here integrated to guide the design of NPs with preferential nano-bio behaviors. Data systematically collected from simulations (or experiments, if available) are first used to train one or more artificial neural networks, each optimized for a specific kind of nano-bio interaction; the trained networks are then interconnected in suitable arrays to obtain the NP core morphology and layer composition that best satisfy all the nano-bio interactions underlying more complex behaviors. This reverse engineering approach is illustrated in the case of NP-membrane interactions, using binding modes and affinities and early stage membrane penetrations as training data. Adaptations for designing NPs with preferential nano-protein interactions and for optimizing solution conditions in the test tube are discussed.